1,1 - difluoro - 2,2 - dichloroethyl difluoromethyl ether and its method of preparation



3,527,812 1,1 DIFLUORO 2,2 DICHLOROETHYL DIFLUO- ROMETHYL ETHER AND ITS METHOD OF PREPARATION Ross C. Terrell, Summit, NJ., assignor to Air Reduction Company, Incorporated, New York, N.Y., a corporation of New York No Drawing. Original application Oct. 3, 1966, Ser. No. 583,948, now Patent No. 3,461,213, dated Aug. 12, 1969. Divided and this application Oct. 9, 1968, Ser. No. 778,904

Int. Cl. C07c 43/00, 43/12 US. Cl. 260-614 1 Claim ABSTRACT OF THE DISCLOSURE This application discloses the. novel compound 1,1- difluoro-2,2-dichloroethyl difiuoromethyl ether having the formula CHF OCF CHCI The compound is prepared by fluorination of the corresponding dichloromethyl ether using fiuorinatingagents in the presence of pentavalent antimony salts or tetravalent halides as fluorination catalysts.'The precursor dichloromethyl ether is prepared by chlorination of the methyl ether. The novel ether has useful anesthetic properties and is a useful solvent.

CROSS-REFERENCE TO RELATED APPLICATION CHClzOCFzCHClz CHF2OCF2CHC12 21101 Fluorinating agents useful in carrying out the above reaction are hydrogen fluoride (HF) and antimony trifluoride (SbF The fiuorination catalysts used comprise pentavalent antimony salts such as SbF SbCl or tetravalent 'stannic halides such as SnCl When SbF is used as the fluorination agent the reaction proceeds advantageously at the boiling point of the product and the product is distilled from the reaction mixture as formed. When hydrogen fluoride is used as fluorination agent the reaction can be carried out at temperatures up to the boiling point of the reaction mixture. Lower temperatures are preferred, as the yields are higher. A temperature of 0l0 C. is preferred.

The use of the above catalysts is required in order to carry out the fluorination effectively. In the absence of such catalysts the fluorinating agents are inoperative. Preferably the catalyst is used in an amount comprising from /2 to by weight (calculated as SbCl of the reaction mixture. Upon completion of the reaction the product is readily separated by distillation.

The precursor dichloromethyl ether employed in the preparation of the new difluoromethyl ether is a new compound. It may advantageously be prepared by chlorination of 1,1-difluoro-2,2-dichloroethyl methyl ether in accordance with the following reaction equation:

CHsOCFzCHClz CHClzOCFzOHClz The chlorination advantageously is carried out at temperatures of -40 C. with the addition of about 1.5 to 2.0 molar equivalents of chlorine. The reaction proceeds readily in the presence of incandescent light to 3,527,812 Patented Sept. 8, 1970 ice yield the desired CHCI OCF CHCI which is used in the subsequent fluorination. The following examples illustrate the preparation of the new compound:

EXAMPLE I Preparation of the intermediate CHCl OCF OHCl To a 3-necked round-bottomed flask fitted with a Dry- Ice condenser, a fritted glass gas inlet tube, a thermometer, and a stirrer, was charged 165 g. (1 mole) of CH OCF CHFCI. After flushing the system with nitrogen, chlorine gas was added via the inlet tube while the reaction was stirred and illuminated with a 300 watt incandescent lamp. The chlorination was rapid and exothermic and the reactor was cooled to hold the temperature between 30 and 35 C. The eflluent gases were led from the top of the condenser to a water scrubber which was titrated at intervals with standard base. When a total of 1.94 moles of HCl per mole of ether was titrated the reaction was stopped. The crude product obtained weighed 224 g. which corresponded to the addition of 1.67 moles of chlorine per mole of the starting ether. The product was flash distilled to yield 215 g. of crude product. Fractional distillation of this mixture using a 60 x 1 cm. column packed with glass helices yielded 74 g. consisting essentially of CHCI OCF CHCI B.P. 5659 C. at 20 mm., 11 1.42631.4283.

Analysis.Calc. for C H F Cl O (percent): C, 15.4; H, 0.86. Found (percent): C, 15.32; H, 0.82.

There was also recovered 25 -g. of the monochlorinated product CH ClOCF CHCl which can be recycled.

EXAMPLE 11 Preparation of OHF OCF CHCI To a mixture of 220 g. CHCI OCF CHCI prepared as described in Example I, and 5.5 g. (2.5% by weight) SbCl was added anhydrous hydrogen fluoride while the temperature was maintained at 0:5 C. The reaction was carried out in a 3-necked stainless steel flask fitted with a stainless steel stirrer, a thermocouple well and a copper Dry-Ice condenser. The amount of hydrogen fluoride added was measured by titration of the HCl given oif. At the end of the reaction the mixture was poured into water and the organic layer (123 g., n 1.3512) recovered. Fractional distillation gave 94 g. of the pure ether CHF OCF CHCI B.P. 87 C., n 1.3484.

Analysis.Calc. (percent): C, 17.93; H, 0.99; F, 37.82. Found (percent): C, 18.08; H, 1.06; F, 37.95.

EXAMPLE III To a stirred mixture of antimony trifluoride (50 g.) and antimony pentafluoride (1 g.) in a stainless steel flask was added a total of 74 g. of CHC1 OCF CHCl The ether was added slowly, keeping the reaction temperature at 100 C. The product was distilled from the reaction mixture as it was formed. The total distillate was washed with cold 2 N base, dried over K CO and distilled to give 27 g. of the desired CHF OCF CHCI 1,1-difluoro-2,2-dichloroethyl difluoromethyl ether is a stable compound. It does not undergo degradation in the presence of alkali or light and has highly advantageous anesthetic properties. This compound is easily miscible with other organic liquids including fats and oils and has useful solvent properties, such as for example as a solvent for fluorinated olefins and other fluorinated materials, such for example as fluorowaxes. It may be used to prepare pastes and dispersions of such materials useful for coatings and the like and may be used as a degreasing agent.

1,1-difluoro-Z,2-dichloroethy1 difluoromethyl ether exhibits anesthetic properties in mammals and is extremely effective for inducing and maintaining anesthesia in laboratory animals, such as mice and dogs, when administered by inhalation. The agent is non-flammable in oxygen. It lends itself to effective use as an inhalant anesthetic in respirable mixtures containing life-supporting concentrations of oxygen. In addition, studies with the agent have shown that it is highly potent, affords good muscular relaxation, is non-toxic, produces minimal irritation and secretions, possesses a high margin of safety, affords rapid induction and recovery, and affords ease of control of levels of anesthesia.

Illustrative of the effectiveness of the agent are the tests conducted with mice in which separate groups of five mice were placed in 1 liter jars previously flushed with oxygen and charged with varying predetermined amounts of the agent. These tests showed the agent to be an effective anesthetic at concentrations as low as 1.25% by volume. The induction time at this concentration was 0.90 minute. At a higher concentration a reduction of induction time occurred, for example, at 2.5% induction occurred in approximately 0.45 minute. After minutes exposure to such respirable atmospheres the test animals were withdrawn and recovered quite promptly, the recovery for example occurring in 2.5 minutes at the 1.25% concentration level and 5.7 minutes at the 2.5% anesthetic level.

The closed system with face mask were employed for administration of the agent in connection with dog anesthesia. Tests were carried out with dogs utilizing an average dose of 0.6-1.0 ml./kg./hr. during a series of /2 hour anesthesias. The mean induction time was 3.2 minutes and the recovery time 9.5 minutes.

It should be understood that the foregoing disclosure References Cited UNITED STATES PATENTS 2,066,905 l/1937 Booth. 2,803,665 8/1957 Miller et al. 2,803,666 8/1957 Miller et a1. 1 3,095,354 6/1963 Larsen et al. 424-366 3,104,202 9/1963 Larsen 424366 3,278,615 10/1966 Larsen et al.

OTHER REFERENCES Mitsch et al., Jour. Heterocyclic Chem., 1965, 2, pp. 152-155. Gubanov et al., Zh. Obshck, Khim., 34 (8), pp. 2802-3,

Clayton et al., Jour. Chem. Soc., 1965, p. 7377.

Hudlicky, Chemistry of Organic Fluorine Compounds, MacMillan Co., New York, (1926), pp. 9197.

LEON ZITVER, Primary Examiner H. T. MARS, Assistant Examiner 

